| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:80220299-80220483 | Common:2; Rare:134; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr17:80260524-80260945 | Common:9; Rare:41 | ||||
| chr17:80415099-80415527 | Common:10; Rare:313 | ||||
| chr17:80544771-80545118 | Common:2; Rare:115 | ||||
| chr17:80545160-80545890 | Common:12; Rare:308 | ||||
| chr17:80991736-80991930 | Common:3; Rare:140 | ||||
| chr17:81034852-81035166 | Common:4; Rare:233 | ||||
| chr17:81083160-81083590 | Common:2; Rare:211 | ||||
| chr17:81097251-81097739 | Common:5; Rare:234 | ||||
| chr17:81165750-81166140 | Rare:246 | ||||
| chr17:81239008-81239410 | Common:8; Rare:270 | ||||
| chr17:81295144-81295433 | Common:4; Rare:126 | ||||
| chr17:81330240-81330670 | Rare:133 | ||||
| chr17:81395149-81395506 | Common:2; Rare:177 | ||||
| chr17:81512735-81513029 | Common:12; Rare:279; Clinvar (benign):14 |